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Eosinophilic granuloma of the orbit: report of two cases.

机译:眼眶嗜酸性肉芽肿:2例报道。

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摘要

We present clinical, radiological, and histopathological findings and treatment results of two infants with orbital eosinophilic granuloma. Both patients presented at 1 year of age with unilateral proptosis, periorbital edema, and a superotemporally located, ill-defined orbital mass on computed tomographic (CT) imaging, with bone erosion in one patient. After subtotal excision, histopathological examination revealed eosinophilic granuloma, and the proptosis resolved with no sign of orbital tumor recurrence or systemic involvement at 12 and 23 months follow-up. Eosinophilic granuloma is a rare childhood orbital tumor that may or may not present with osteolytic change.
机译:我们介绍了两名婴儿眼眶嗜酸性粒细胞肉芽肿的临床,影像学和组织病理学发现及治疗结果。两名患者均在1岁时出现单侧眼球突出,眶周水肿,并且在计算机断层扫描(CT)成像中眼眶位置临时定位,边界不清,一名患者出现骨质侵蚀。大体切除后,组织病理学检查显示嗜酸性肉芽肿,并且在术后12和23个月的随访中,眼球突出消失,无眼眶肿瘤复发或全身受累的迹象。嗜酸性肉芽肿是一种罕见的儿童眼眶肿瘤,可能会或可能不会出现溶骨性改变。

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